小麦与真菌相互作用中lncrna的功能分化:来自茎锈病应答小麦转录组的见解。

IF 3.3 3区 生物学 Q1 PLANT SCIENCES
S Jyothsna, Minu M Nair, Manickavelu Alagu
{"title":"小麦与真菌相互作用中lncrna的功能分化:来自茎锈病应答小麦转录组的见解。","authors":"S Jyothsna, Minu M Nair, Manickavelu Alagu","doi":"10.1007/s12298-025-01599-x","DOIUrl":null,"url":null,"abstract":"<p><p>Stem rust of wheat, caused by the fungal pathogen <i>Puccinia graminis</i> f. sp. <i>tritici</i> (<i>Pgt</i>), is an economically significant disease affecting wheat production globally. The recent progress in high-throughput sequencing technology has uncovered the crucial role of non-coding RNAs, an emerging yet influential regulatory genetic element modulating plant response against abiotic and biotic stresses. Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) are prominent regulatory nRNAs, renowned for their ability to finely tune plant gene expression across transcriptional, post-transcriptional, and epigenetic layers. The current study adopts a comprehensive transcriptome sequencing approach to identify stem rust-responsive lncRNAs from near isogenic lines of wheat introgressed with resistance gene <i>Sr36</i>, along with their susceptible variety, HD2329. A meticulous lncRNA selection criterion yielded a total of 948 <i>Pgt</i>-responsive lncRNAs. The detection of 11 lncRNAs acting as miRNA precursors, along with 590 miRNA-lncRNA target interactions further highlights the dynamic interplay between miRNAs and lncRNAs during <i>Pgt</i> infection in wheat. Moreover, the functional annotation of lncRNA targets unveiled the prevalence of genes such as LRR receptor-like serine/threonine-protein kinases, disease resistance protein RPM1-like, chitin elicitor receptor kinase, nudix hydrolases and NAC transcription factors, that are involved in discrete biological pathways crucial for plant stress responses. Detection of 37 SSR marker-bearing lncRNAs along with the interaction of lncRNAs with disease-associated transcription factors such as C2H2, ERF, GATA and Dof, further elevate the significance of the study. The study unveils potential functional divergence within lncRNAs and serves as a fine resource that can be harnessed to elucidate the interplay of coding and non-coding RNAs governing wheat-fungal interactions.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s12298-025-01599-x.</p>","PeriodicalId":20148,"journal":{"name":"Physiology and Molecular Biology of Plants","volume":"31 5","pages":"709-727"},"PeriodicalIF":3.3000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12185806/pdf/","citationCount":"0","resultStr":"{\"title\":\"Functional divergence of LncRNAs in wheat-fungal interactions: insights from stem rust-responsive wheat transcriptomes.\",\"authors\":\"S Jyothsna, Minu M Nair, Manickavelu Alagu\",\"doi\":\"10.1007/s12298-025-01599-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Stem rust of wheat, caused by the fungal pathogen <i>Puccinia graminis</i> f. sp. <i>tritici</i> (<i>Pgt</i>), is an economically significant disease affecting wheat production globally. The recent progress in high-throughput sequencing technology has uncovered the crucial role of non-coding RNAs, an emerging yet influential regulatory genetic element modulating plant response against abiotic and biotic stresses. Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) are prominent regulatory nRNAs, renowned for their ability to finely tune plant gene expression across transcriptional, post-transcriptional, and epigenetic layers. The current study adopts a comprehensive transcriptome sequencing approach to identify stem rust-responsive lncRNAs from near isogenic lines of wheat introgressed with resistance gene <i>Sr36</i>, along with their susceptible variety, HD2329. A meticulous lncRNA selection criterion yielded a total of 948 <i>Pgt</i>-responsive lncRNAs. The detection of 11 lncRNAs acting as miRNA precursors, along with 590 miRNA-lncRNA target interactions further highlights the dynamic interplay between miRNAs and lncRNAs during <i>Pgt</i> infection in wheat. Moreover, the functional annotation of lncRNA targets unveiled the prevalence of genes such as LRR receptor-like serine/threonine-protein kinases, disease resistance protein RPM1-like, chitin elicitor receptor kinase, nudix hydrolases and NAC transcription factors, that are involved in discrete biological pathways crucial for plant stress responses. Detection of 37 SSR marker-bearing lncRNAs along with the interaction of lncRNAs with disease-associated transcription factors such as C2H2, ERF, GATA and Dof, further elevate the significance of the study. The study unveils potential functional divergence within lncRNAs and serves as a fine resource that can be harnessed to elucidate the interplay of coding and non-coding RNAs governing wheat-fungal interactions.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s12298-025-01599-x.</p>\",\"PeriodicalId\":20148,\"journal\":{\"name\":\"Physiology and Molecular Biology of Plants\",\"volume\":\"31 5\",\"pages\":\"709-727\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12185806/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physiology and Molecular Biology of Plants\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s12298-025-01599-x\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/15 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiology and Molecular Biology of Plants","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s12298-025-01599-x","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/15 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

小麦茎锈病是一种影响全球小麦生产的重大经济病害,是由小麦锈病(Pgt)引起的。近年来,高通量测序技术的进展揭示了非编码rna在植物对非生物和生物胁迫反应中的重要作用,非编码rna是一种新兴但有影响力的调控遗传元件。长链非编码rna (lncRNAs)和微rna (miRNAs)是重要的调控rna,以其在转录、转录后和表观遗传层精细调节植物基因表达的能力而闻名。目前的研究采用全面的转录组测序方法,从导入抗性基因Sr36的小麦近等基因系及其易感品种HD2329中鉴定茎锈病响应的lncrna。细致的lncRNA选择标准共产生948个pgt响应的lncRNA。检测到11种lncrna作为miRNA前体,以及590种miRNA- lncrna靶标相互作用,进一步强调了小麦Pgt感染过程中miRNA和lncrna之间的动态相互作用。此外,lncRNA靶点的功能注释揭示了LRR受体样丝氨酸/苏氨酸蛋白激酶、抗病蛋白rpm1样、几丁质激发子受体激酶、裸酶水解酶和NAC转录因子等基因的普遍存在,这些基因参与了对植物胁迫应答至关重要的离散生物学途径。检测到37个带有SSR标记的lncrna,以及lncrna与C2H2、ERF、GATA、Dof等疾病相关转录因子的相互作用,进一步提升了研究的意义。该研究揭示了lncrna内部潜在的功能差异,并为阐明编码rna和非编码rna调控小麦与真菌相互作用的相互作用提供了良好的资源。补充信息:在线版本包含补充资料,提供地址为10.1007/s12298-025-01599-x。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional divergence of LncRNAs in wheat-fungal interactions: insights from stem rust-responsive wheat transcriptomes.

Stem rust of wheat, caused by the fungal pathogen Puccinia graminis f. sp. tritici (Pgt), is an economically significant disease affecting wheat production globally. The recent progress in high-throughput sequencing technology has uncovered the crucial role of non-coding RNAs, an emerging yet influential regulatory genetic element modulating plant response against abiotic and biotic stresses. Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) are prominent regulatory nRNAs, renowned for their ability to finely tune plant gene expression across transcriptional, post-transcriptional, and epigenetic layers. The current study adopts a comprehensive transcriptome sequencing approach to identify stem rust-responsive lncRNAs from near isogenic lines of wheat introgressed with resistance gene Sr36, along with their susceptible variety, HD2329. A meticulous lncRNA selection criterion yielded a total of 948 Pgt-responsive lncRNAs. The detection of 11 lncRNAs acting as miRNA precursors, along with 590 miRNA-lncRNA target interactions further highlights the dynamic interplay between miRNAs and lncRNAs during Pgt infection in wheat. Moreover, the functional annotation of lncRNA targets unveiled the prevalence of genes such as LRR receptor-like serine/threonine-protein kinases, disease resistance protein RPM1-like, chitin elicitor receptor kinase, nudix hydrolases and NAC transcription factors, that are involved in discrete biological pathways crucial for plant stress responses. Detection of 37 SSR marker-bearing lncRNAs along with the interaction of lncRNAs with disease-associated transcription factors such as C2H2, ERF, GATA and Dof, further elevate the significance of the study. The study unveils potential functional divergence within lncRNAs and serves as a fine resource that can be harnessed to elucidate the interplay of coding and non-coding RNAs governing wheat-fungal interactions.

Supplementary information: The online version contains supplementary material available at 10.1007/s12298-025-01599-x.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.10
自引率
0.00%
发文量
126
期刊介绍: Founded in 1995, Physiology and Molecular Biology of Plants (PMBP) is a peer reviewed monthly journal co-published by Springer Nature. It contains research and review articles, short communications, commentaries, book reviews etc., in all areas of functional plant biology including, but not limited to plant physiology, biochemistry, molecular genetics, molecular pathology, biophysics, cell and molecular biology, genetics, genomics and bioinformatics. Its integrated and interdisciplinary approach reflects the global growth trajectories in functional plant biology, attracting authors/editors/reviewers from over 98 countries.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信